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BMC Microbiology|May 28, 2020
Effect of donor-recipient relatedness on the plasmid conjugation frequency: a meta-analysisJesse B Alderliesten, Sarah J N Duxbury, Mark P Zwart, et al.Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.Proceedings. Biological Sciences|November 3, 2021
Chicken gut microbiome members limit the spread of an antimicrobial resistance plasmid in Escherichia coliSarah J N Duxbury, Jesse B Alderliesten, Mark P Zwart, et al.Annals of Neurology|October 1, 1996
Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathiesP H Meijerink, J E Hoogendijk, A A Gabreëls-Festen, et al.Plos One|April 15, 2016
Lineage Tracking for Probing Heritable Phenotypes at Single-Cell ResolutionDenis Cottinet, Florence Condamine, Nicolas Bremond, et al.Journal of Neurology|December 4, 2003
The spectrum of lower motor neuron syndromesR M Van Den Berg-Vos, L H Van Den Berg, J Visser, et al.Human Molecular Genetics|May 18, 2000
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)A Muchir, G Bonne, A J van der Kooi, et al.European Journal of Neurology|December 18, 2008
Degenerative cervical radiculopathy: diagnosis and conservative treatment. A reviewB Kuijper, J Th J Tans, R J Schimsheimer, et al.Lab on a Chip|October 21, 2011
Millifluidic droplet analyser for microbiologyLarysa Baraban, Fabien Bertholle, Merijn L M Salverda, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 23, 2000
Extension of the clinical range of facioscapulohumeral dystrophy: report of six casesA J van der Kooi, M C Visser, N Rosenberg, et al.Pageof 25